Mean Change From Baseline in Hemoglobin A1c (HbA1c) (10 mg and 15 mg)
| Group | Value (Percentage of HbA1c) | Spread |
|---|---|---|
| 10 mg Tirzepatide | -2.44 | 0.073 |
| 15 mg Tirzepatide | -2.49 | 0.072 |
| Insulin Glargine | -0.95 | 0.073 |
Trial · Interventional
CompletedPhase 3Results postedRegistry dataAustralia, China, India, South Korea
1 trial · 1 completed · 1 with posted results
A Study of Tirzepatide (LY3298176) in Participants With Type 2 Diabetes on Metformin With or Without Sulfonylurea (SURPASS-AP-Combo)
NCT040937529 Dec 2019 to 24 Nov 2021
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
The main reason for this study is to compare the study drug tirzepatide to insulin glargine in participants with type 2 diabetes on metformin with or without a sulfonylurea.
Experimental
5 mg Tirzepatide
Participants received 5 milligrams (mg) tirzepatide administered subcutaneously (SC) once weekly (QW).
Experimental
10 mg Tirzepatide
Participants received 10 mg tirzepatide administered SC QW.
Experimental
15 mg Tirzepatide
Participants received 15 mg tirzepatide administered SC QW.
Active comparator
Insulin Glargine
Participants received insulin glargine administered once daily (QD) SC. The starting dose of insulin glargine was 6 Insulin Units (IU)/day at bedtime, titrated to a fasting blood glucose (FBG) between 72-100 milligrams per Deciliter (mg/dL), following a treat-to-target (TTT) algorithm.
Outcomes the sponsor listed as primary.
Mean Change From Baseline in Hemoglobin A1c (HbA1c) (10 mg and 15 mg)
Time frame · Baseline, Week 40
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Least Squares (LS) mean was determined by mixed model repeated measures (MMRM) model with covariates Baseline + Country + Baseline Oral Antihyperglycemic Medication (OAM) Use (Metformin (Met), Met plus Sulfonylurea (SU)) + Treatment + Time + Treatment\*Time (Type III sum of squares).
Mean Change From Baseline in HbA1c (5 mg)
Time frame · Baseline, Week 40
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. LS mean was determined by MMRM model with covariates Baseline + Country + Baseline OAM Use (Met, Met plus SU) + Treatment + Time + Treatment\*Time (Type III sum of squares).
Mean Change From Baseline in Body Weight
Time frame · Baseline, Week 40
LS mean was determined by MMRM model with Baseline + Country + Baseline OAM Use (Met, Met plus SU) + Baseline HbA1c Group (\<= 8.5%, \>8.5%) + Treatment + Time + Treatment\*Time (Type III sum of squares) as covariates.
Percentage of Participants Achieving an HbA1c Target Value of <7.0%
Time frame · Week 40
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured to identify average plasma glucose concentration over prolonged periods of time. Imputed data includes observed value and imputed value if endpoint measure is missing.
Percentage of Participants Achieving an HbA1c Target Value of <5.7%
Time frame · Week 40
HbA1c is the glycosylated fraction of hemoglobin A. Imputed data includes observed value and imputed value if endpoint measure is missing.
Mean Change From Baseline in Fasting Serum Glucose
Time frame · Baseline, Week 40
Fasting serum glucose (FSG) is a test to determine sugar levels in serum sample after an overnight fast. LS mean was determined by MMRM model with Baseline + Country + Baseline OAM Use (Met, Met plus SU) + Baseline HbA1c Group (\<= 8.5%, \>8.5%) + Treatment + Time + Treatment\*Time (Type III sum of squares) as covariates.
Mean Change in Daily Glucose Average From Baseline in 7-Point Self-Monitored Blood Glucose (SMBG) Values
Time frame · Baseline, Week 40
The SMBG data was collected at the following 7 time points: Morning Premeal - Fasting, Morning 2-hour Post-meal, Midday Premeal, Midday 2-hour Post-meal, Evening Premeal, Evening 2-hour Post-meal and Bedtime. LS mean was determined by MMRM model with Baseline + Country + Baseline OAM Use (Met, Met plus SU) + Baseline HbA1c Group (\<= 8.5%, \>8.5%) + Treatment + Time + Treatment\*Time (Type III sum of squares) as covariates.
Percentage of Participants Who Achieved Weight Loss ≥5%
Time frame · Week 40
Imputed data includes observed value and imputed value if endpoint measure is missing.
Diabetes Treatment Satisfaction as Measured by the Diabetes Treatment Satisfaction Questionnaire, Change Version (DTSQc) Hyperglycemia, Hypoglycemia and Treatment Satisfaction Score
Time frame · Baseline, Week 40
DTSQc, an 8-item questionnaire, assesses relative change in treatment satisfaction perceived frequency of hyperglycemia, and perceived frequency of hypoglycemia from baseline to week 40 or early termination. The treatment satisfaction score ranges from -18 to 18 where the higher the score the greater the improvement in satisfaction with treatment. The lower the score the greater the deterioration in satisfaction with treatment. The hyperglycemia and hypoglycemia scores range from -3 to 3 where negative scores indicate fewer problems with blood glucose levels and positive scores indicate more problems than before. LS mean was determined by ANCOVA model for endpoint measures with Baseline + Country + Baseline HbA1c Group (\<=8.5%, \>8.5%) + Baseline OAM Use (Met, Met plus SU) + Treatment (Type III sum of squares) as covariates.
Rate of Hypoglycemia With Blood Glucose < 54 mg/dL or Severe Hypoglycemia
Time frame · Baseline through end of safety follow-up (Up To Week 44)
The hypoglycemia events were defined by participant reported events with blood glucose \< 54 mg/dL \[\<3.0 Millimole per Liter (mmol/L)\] or severe hypoglycemia. Severe hypoglycemia is defined as an episode with severe cognitive impairment requiring the assistance of another person to actively administer carbohydrate, glucagon, or other resuscitative actions. These episodes may be associated with sufficient neuroglycopenia to induce seizure or coma. The rate of post-baseline hypoglycemia was estimated by negative binomial model: Number of episodes = Country + Baseline OAM Use (Met, Met plus SU) + Baseline HbA1c Group (\<= 8.5%, \>8.5%) + Treatment, with log (exposure in days/365.25) as an offset variable.
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (Percentage of HbA1c) | Spread |
|---|---|---|
| 10 mg Tirzepatide | -2.44 | 0.073 |
| 15 mg Tirzepatide | -2.49 | 0.072 |
| Insulin Glargine | -0.95 | 0.073 |
| Group | Value (Percentage of HbA1c) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -2.24 | 0.070 |
| Insulin Glargine | -0.95 | 0.073 |
| Group | Value (kilograms (kg)) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -5.0 | 0.32 |
| 10 mg Tirzepatide | -7.0 | 0.33 |
| 15 mg Tirzepatide | -7.2 | 0.33 |
| Insulin Glargine | 1.5 | 0.33 |
| Group | Value (Percentage of participants) |
|---|---|
| 5 mg Tirzepatide | 75.44 |
| 10 mg Tirzepatide | 86.04 |
| 15 mg Tirzepatide | 84.38 |
| Insulin Glargine | 23.72 |
| Group | Value (Percentage of participants) |
|---|---|
| 5 mg Tirzepatide | 14.91 |
| 10 mg Tirzepatide | 20.72 |
| 15 mg Tirzepatide | 27.68 |
| Insulin Glargine | 0.00 |
| Group | Value (milligrams per deciliter (mg/dL)) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -58.6 | 2.13 |
| 10 mg Tirzepatide | -66.2 | 2.19 |
| 15 mg Tirzepatide | -64.8 | 2.19 |
| Insulin Glargine | -46.2 | 2.19 |
| Group | Value (milligrams per deciliter (mg/dL)) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -77.0 | 2.09 |
| 10 mg Tirzepatide | -83.4 | 2.16 |
| 15 mg Tirzepatide | -84.6 | 2.18 |
| Insulin Glargine | -42.8 | 2.18 |
| Group | Value (Percentage of participants) |
|---|---|
| 5 mg Tirzepatide | 55.70 |
| 10 mg Tirzepatide | 71.62 |
| 15 mg Tirzepatide | 74.11 |
| Insulin Glargine | 5.58 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| 5 mg TirzepatideParticipants received 5 mg tirzepatide administered SC QW. | 0 / 230 | 15 / 230 | 174 / 230 |
| 10 mg TirzepatideParticipants received 10 mg tirzepatide administered SC QW. | 0 / 228 | 14 / 228 | 201 / 228 |
| 15 mg TirzepatideParticipants received 15 mg tirzepatide administered SC QW. | 1 / 229 | 15 / 229 | 193 / 229 |
| Insulin GlargineParticipants received insulin glargine administered QD SC. The starting dose of insulin glargine was 6 IU/day at bedtime, titrated to a FBG between 72-100 mg/dL, following a TTT algorithm. | 2 / 220 | 20 / 220 | 83 / 220 |
Each cell reads participants affected / participants at risk, as the registry posted them.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies that cite this trial.
1 study on this page
Indexing hint: Randomized controlled trial · 2023
Gao et al. 2023Nature medicinecited by 80
PMID 37231074DOI 10.1038/s41591-023-02344-1PUB-37231074
1 study on this page
PubMed tag: none · 2024
Bi et al. 2024Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 6
PMID 38494574PMC11043231DOI 10.1007/s13300-024-01561-2PUB-38494574
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